Variant report

Variant	rs7704088
Chromosome Location	chr5:37139805-37139806
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs16903412	1.00[YRI][hapmap]
rs16903524	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16903527	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs16903598	1.00[AMR][1000 genomes]
rs16903600	1.00[AMR][1000 genomes]
rs16903603	1.00[AMR][1000 genomes]
rs16903604	1.00[AMR][1000 genomes]
rs34243761	1.00[AMR][1000 genomes]
rs56725398	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57564262	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58089157	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58132646	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58498167	1.00[AMR][1000 genomes]
rs59150742	1.00[AMR][1000 genomes]
rs59775401	1.00[AMR][1000 genomes]
rs60290055	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60570427	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61005381	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61062002	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61561054	1.00[AMR][1000 genomes]
rs61732654	1.00[AMR][1000 genomes]
rs6863554	1.00[AMR][1000 genomes]
rs73066405	1.00[AMR][1000 genomes]
rs73068410	1.00[AMR][1000 genomes]
rs73068415	1.00[AMR][1000 genomes]
rs73068449	1.00[AMR][1000 genomes]
rs73093847	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73093898	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095712	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095713	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095726	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095728	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095735	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095736	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73095753	1.00[AMR][1000 genomes]
rs73095756	1.00[AMR][1000 genomes]
rs7720731	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7727585	1.00[AMR][1000 genomes]
rs7728924	1.00[YRI][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	esv1802391	chr5:36958598-37242600	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv597822	chr5:36997953-37147152	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv534064	chr5:37054962-37586210	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
10	nsv881511	chr5:37088627-37552852	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
11	nsv597823	chr5:37111565-37430365	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
12	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
13	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
14	nsv1025988	chr5:37115142-37586211	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv537727	chr5:37115142-37586211	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37082800-37169200	Weak transcription	Spleen	Spleen
2	chr5:37103800-37143200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:37105800-37156200	Weak transcription	NHLF	lung
4	chr5:37106000-37143400	Weak transcription	HepG2	liver
5	chr5:37106200-37150200	Weak transcription	NHEK	skin
6	chr5:37108200-37143800	Weak transcription	Gastric	stomach
7	chr5:37112200-37198200	Weak transcription	Small Intestine	intestine
8	chr5:37112800-37142800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr5:37113600-37222200	Weak transcription	Psoas Muscle	Psoas
10	chr5:37113800-37157000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr5:37114600-37165400	Weak transcription	HMEC	breast
12	chr5:37116200-37142200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr5:37118600-37153600	Weak transcription	Pancreas	Pancrea
14	chr5:37122000-37156000	Weak transcription	Brain Substantia Nigra	brain
15	chr5:37122200-37143600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr5:37122800-37150800	Weak transcription	Fetal Heart	heart
17	chr5:37124200-37149400	Weak transcription	NH-A	brain
18	chr5:37133200-37140000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:37133200-37169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr5:37133600-37144000	Strong transcription	HSMM	muscle
21	chr5:37134200-37171200	Weak transcription	Colonic Mucosa	Colon
22	chr5:37135000-37143200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:37135400-37140000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr5:37135400-37140200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr5:37135400-37146200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:37136000-37141400	Strong transcription	Left Ventricle	heart
27	chr5:37136200-37197200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr5:37136800-37143400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:37136800-37170000	Weak transcription	Esophagus	oesophagus
30	chr5:37137000-37140600	Weak transcription	Lung	lung
31	chr5:37137000-37143000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:37137000-37145800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr5:37137200-37143600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr5:37137200-37143600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:37137200-37143800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:37137200-37143800	Strong transcription	Fetal Thymus	thymus
37	chr5:37137400-37174000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr5:37137600-37169000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr5:37137800-37141400	Strong transcription	Fetal Muscle Leg	muscle
40	chr5:37137800-37141800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr5:37137800-37143000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:37137800-37143400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:37137800-37143600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:37137800-37143800	Weak transcription	Fetal Intestine Small	intestine
45	chr5:37138000-37140600	Weak transcription	Stomach Smooth Muscle	stomach
46	chr5:37138000-37142200	Weak transcription	Primary B cells from peripheral blood	blood
47	chr5:37138000-37143200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr5:37138000-37143600	Weak transcription	Duodenum Mucosa	Duodenum
49	chr5:37138000-37143600	Weak transcription	Fetal Stomach	stomach
50	chr5:37138000-37150200	Weak transcription	Primary T cells from cord blood	blood

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